Canonical Allele Identifier: PA658665229
Gene: SOX9 HGNC NCBI

Linked Data

ClinVar Variation Id: 451006
ClinVar RCV Id: RCV000520332 RCV001378337
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000337.1:p.Pro176Arg
CA400866496
NM_000346.4:c.527C>G